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Section 50.1
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Definitions |
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Section 50.3
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General requirements for informed consent |
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Section 50.20
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Exception from general requirements |
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Section 50.23
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Exception from informed consent requirements for emergency research |
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Section 50.24
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Elements of informed consent |
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Section 50.25
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Documentation of informed consent |
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Section 50.27
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IRB duties |
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Section 50.50
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Clinical investigations not involving greater than minimal risk |
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Section 50.51
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Clinical investigations involving greater than minimal risk but presenting the prospect of direct benefit to individual |
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Section 50.52
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Clinical investigations involving greater than minimal risk and no prospect of direct benefit to individual subjects, but likely to yield generalizable knowledge about the subjects' disorder or |
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Section 50.53
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Clinical investigations not otherwise approvable that present an opportunity to understand, prevent, or alleviate a serious problem affecting the health or welfare of children |
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Section 50.54
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Requirements for permission by parents or guardians and for assent by children |
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Section 50.55
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Wards |
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Section 50.56
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Purpose |